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Andreas Heine

Showing results (61-70 of 134) with videos related to

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Journal of Medicinal Chemistry|January 23, 2004
Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognitionAlexander Weber, Angela Casini, Andreas Heine, et al.
Bioorganic & Medicinal Chemistry|December 7, 2002
Structure-based mutagenesis approaches toward expanding the substrate specificity of D-2-deoxyribose-5-phosphate aldolaseGrace DeSantis, Junjie Liu, David P Clark, et al.
Journal of Molecular Biology|May 14, 2003
Structural basis for antibody catalysis of a cationic cyclization reactionXueyong Zhu, Andreas Heine, Frédéric Monnat, et al.
Bioorganic & Medicinal Chemistry|September 2, 2008
Achiral oligoamines as versatile tool for the development of aspartic protease inhibitorsAndreas Blum, Jark Böttcher, Benedikt Sammet, et al.
Journal of Medicinal Chemistry|June 24, 2014
Chasing protons: how isothermal titration calorimetry, mutagenesis, and pKa calculations trace the locus of charge in ligand binding to a tRNA-binding enzymeManuel Neeb, Paul Czodrowski, Andreas Heine, et al.
ACS Chemical Biology|December 14, 2016
Elucidating the Origin of Long Residence Time Binding for Inhibitors of the Metalloprotease ThermolysinJonathan Cramer, Stefan G Krimmer, Veronica Fridh, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 21, 2011
Stereo- and regioselective azide/alkyne cycloadditions in carbonic anhydrase II via tethering, monitored by crystallography and mass spectrometryJohannes Schulze Wischeler, Dong Sun, Nicola U Sandner, et al.
Bioorganic & Medicinal Chemistry|April 3, 2003
Directed evolution of N-acetylneuraminic acid aldolase to catalyze enantiomeric aldol reactionsMasaru Wada, Che-Chang Hsu, Dirk Franke, et al.
Angewandte Chemie (International Ed. in English)|August 21, 2007
Saccharin inhibits carbonic anhydrases: possible explanation for its unpleasant metallic aftertasteKaren Köhler, Alexander Hillebrecht, Johannes Schulze Wischeler, et al.
Angewandte Chemie (International Ed. in English)|April 12, 2005
An old target revisited: two new privileged skeletons and an unexpected binding mode for HIV-protease inhibitorsEdgar Specker, Jark Böttcher, Hauke Lilie, et al.
Pageof 14

Showing results (61-70 of 134) with videos related to

Sort By:
Pageof 14
Journal of Medicinal Chemistry|January 23, 2004
Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognitionAlexander Weber, Angela Casini, Andreas Heine, et al.
Bioorganic & Medicinal Chemistry|December 7, 2002
Structure-based mutagenesis approaches toward expanding the substrate specificity of D-2-deoxyribose-5-phosphate aldolaseGrace DeSantis, Junjie Liu, David P Clark, et al.
Journal of Molecular Biology|May 14, 2003
Structural basis for antibody catalysis of a cationic cyclization reactionXueyong Zhu, Andreas Heine, Frédéric Monnat, et al.
Bioorganic & Medicinal Chemistry|September 2, 2008
Achiral oligoamines as versatile tool for the development of aspartic protease inhibitorsAndreas Blum, Jark Böttcher, Benedikt Sammet, et al.
Journal of Medicinal Chemistry|June 24, 2014
Chasing protons: how isothermal titration calorimetry, mutagenesis, and pKa calculations trace the locus of charge in ligand binding to a tRNA-binding enzymeManuel Neeb, Paul Czodrowski, Andreas Heine, et al.
ACS Chemical Biology|December 14, 2016
Elucidating the Origin of Long Residence Time Binding for Inhibitors of the Metalloprotease ThermolysinJonathan Cramer, Stefan G Krimmer, Veronica Fridh, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 21, 2011
Stereo- and regioselective azide/alkyne cycloadditions in carbonic anhydrase II via tethering, monitored by crystallography and mass spectrometryJohannes Schulze Wischeler, Dong Sun, Nicola U Sandner, et al.
Bioorganic & Medicinal Chemistry|April 3, 2003
Directed evolution of N-acetylneuraminic acid aldolase to catalyze enantiomeric aldol reactionsMasaru Wada, Che-Chang Hsu, Dirk Franke, et al.
Angewandte Chemie (International Ed. in English)|August 21, 2007
Saccharin inhibits carbonic anhydrases: possible explanation for its unpleasant metallic aftertasteKaren Köhler, Alexander Hillebrecht, Johannes Schulze Wischeler, et al.
Angewandte Chemie (International Ed. in English)|April 12, 2005
An old target revisited: two new privileged skeletons and an unexpected binding mode for HIV-protease inhibitorsEdgar Specker, Jark Böttcher, Hauke Lilie, et al.
Pageof 14